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A Case of Sjogren-Larsson Syndrome

Shin WK, Ohn YH, Park SH, Shin HH

  • KMID: 2205128
  • J Korean Ophthalmol Soc.
  • 1995 Sep;36(9):1605-1609.
The Sjogren-Larsson syndrome is genetically determined syndrome with autosomal recessive inheritence and characterized by the three cardinal signs: congenital ichthyosis, spastic di/tetraplegia, and mental retardation. Ocular signs include ectropion, blepharitis,...
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A Case of Sjogren-Larsson Syndrome

Lee JH, Lee J, Choi GS, Koo SW, Kim YK

  • KMID: 2230539
  • Korean J Dermatol.
  • 1998 Dec;36(6):1078-1082.
Sjogren-Larsson syndrome is a rare autosomal recessive neurocutaneous disorder due to a deficiency of the fatty aldehyde dehydrogenase. It consists of ichthyosis, spastic di- or quardriplegia and mental retardation. We...
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A Case of Sjogren-Larsson Syndrome

Lee KJ, Kim JB, Lee DH, Shin SM, Lee SJ

  • KMID: 1879519
  • J Korean Pediatr Soc.
  • 1994 Dec;37(12):1757-1761.
Sjogren-Larsson Syndrome is a rare disorder chracterized by congenital icthyosis, spastic diplegia or tetraplegia and mental retardation. The inheritance is autosomal recessive, due to deficiency of alcohol dehydrogenase activity of...
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A Case of Sjögren-Larsson Syndrome

Lee HJ, Shim DT, Kim YK, Jin SY

Sjögren-Larsson syndrome(SLS) is a rare hereditable disease characterized by congenital ichthyosis, spastic diplegia and mental retardation. Along with the typical triad of symptoms, many patients with this disease have short...
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A rare case of Sjogren-Larsson syndrome with recurrent pneumonia and asthma

Tavasoli A, Sayyahfar , Behnam B

Sjogren-Larsson syndrome (SLS) is a rare autosomal recessive neurocutaneous disorder with worldwide incidence of 0.4 per 100,000 people. It is characterized by the triad of congenital ichthyosis, spastic diplegia or...
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Identification of Homozygous Likely Pathogenic Variant of ALDH3A2 in a Korean Boy with Sjögren-Larsson Syndrome

Kim JY, Kim SH, Park MJ, Kim SH, Cho WH, Choi J, Ki CS, You SJ

No abstract available.
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